Abstract:The electrochemical carbon dioxide reduction reaction (CO2RR) to C2 chemicals has received great attention. Here, we report the cuprous oxide (Cu2O) nanocubes cooperated with silver (Ag) nanoparticles via the replacement reaction for a synergetic CO2RR. The Cu2O-Ag tandem catalyst exhibits an impressive Faradaic efficiency (FE) of 72.85% for C2 products with a partial current density of 243.32 mA·cm−2. The electrochemical experiments and density functional theory (DFT) calculations reveal that the introduction… Show more
“…Loading Au, Ag, Zn, and other common metal catalysts on Cu has been verified to be effective in producing C 2+ products. 185,[193][194][195][196][197] Jaramillo's group deposited Au on a polycrystalline copper foil and found that the bimetallic Au/ Cu electrocatalyst had much higher activity and selectivity for the formation of C 2+ than that over gold and copper. The formation of products containing C-C bonds on bimetallic Au/Cu was 100 times more selective than C 1 products (methane or methanol) (Fig.…”
Section: Surface Co*(co) Population Controlmentioning
The global warming problem due to greenhouse gases (GHGs), mainly CO2, appears to be a serious concern in our global society. Electrocatalytic CO2 conversion provides an environment-friendly approach to reduce...
“…Loading Au, Ag, Zn, and other common metal catalysts on Cu has been verified to be effective in producing C 2+ products. 185,[193][194][195][196][197] Jaramillo's group deposited Au on a polycrystalline copper foil and found that the bimetallic Au/ Cu electrocatalyst had much higher activity and selectivity for the formation of C 2+ than that over gold and copper. The formation of products containing C-C bonds on bimetallic Au/Cu was 100 times more selective than C 1 products (methane or methanol) (Fig.…”
Section: Surface Co*(co) Population Controlmentioning
The global warming problem due to greenhouse gases (GHGs), mainly CO2, appears to be a serious concern in our global society. Electrocatalytic CO2 conversion provides an environment-friendly approach to reduce...
The field of electrochemical
carbon dioxide reduction has developed
rapidly during recent years. At the same time, the role of the anodic
half-reaction has received considerably less attention. In this Perspective,
we scrutinize the reports on the best-performing CO
2
electrolyzer
cells from the past 5 years, to shed light on the role of the anodic
oxygen evolution catalyst. We analyze how different cell architectures
provide different local chemical environments at the anode surface,
which in turn determines the pool of applicable anode catalysts. We
uncover the factors that led to either a strikingly high current density
operation or an exceptionally long lifetime. On the basis of our analysis,
we provide a set of criteria that have to be fulfilled by an anode
catalyst to achieve high performance. Finally, we provide an outlook
on using alternative anode reactions (alcohol oxidation is discussed
as an example), resulting in high-value products and higher energy
efficiency for the overall process.
“…Moreover, the partial current densities of multicarbon products and oxygenates from CO reduction are higher than those from direct CO 2 reduction on Cu catalysts. For instance, the highest partial current density of n -propanol from CO reduction on a nitrogen-doped graphene quantum dot-decorated Cu nanorod catalyst was 82 mA·cm –2 at −1.5 V vs SHE, while that from CO 2 reduction was 21 mA·cm –2 at −1.7 V vs SHE. , Therefore, a tandem catalyst combining the most active catalyst for CO 2 to CO conversion, such as Au, , Ag, − Zn, , and 3d metal single-atom catalyst, , with a Cu-based catalyst for further reduction of CO is promising to exhibit a high current density of highly reduced products from CO 2 reduction at a relatively positive potential on the SHE scale.…”
Electrochemical reduction of CO2 to high-value
hydrocarbons
and oxygenates is an attractive technique to store intermittent renewable
energy. Diverse catalysts are capable of catalyzing the CO2 to CO conversion, while further reduction of CO occurs almost exclusively
on Cu. Monocomponent Cu catalysts suffer from the high overpotential
and low Faradaic efficiency of hydrocarbons and oxygenates. Combining
CO2 to CO conversion on Au, Ag, single-atom catalysts,
etc., with CO reduction on Cu is a promising strategy to achieve high
selectivity and a high formation rate of highly reduced products.
Numerous tandem catalysts have been developed based on this idea,
and the mass transport of a CO intermediate from a CO-formation catalyst
to Cu is the key factor that needs to be considered in the design
of tandem catalysts. Rational analysis of the different modes of CO
mass transport in the reported designs is needed for further development
of tandem catalysts for CO2 reduction. In this review,
we elucidate how the spatial distribution of the CO-formation catalyst
and Cu determines the mode of CO mass transport and consequently affects
the utilization efficiency and reduction rate of the CO intermediate.
We also discuss the challenges and perspectives in understanding the
interaction between the CO-formation catalyst and Cu and improving
their catalytic performance in the CO2 tandem reduction.
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